HP Hood LLC Recall: Product may contain foreign objects (plastic).

🇺🇸 United States

1. October 25, 2022 - Recall initiated
2. November 9, 2022 - Reported by source
3. March 1, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0121-2023

Event ID

91053

Status

Terminated

Classification

Class II

Company

HP Hood LLC

Product description

Food Club Cottage Cheese with Pineapple, 16 oz; Hannaford Cottage Cheese with Pineapple, 16 oz; Hood Cottage Cheese with Pineapple, 16 oz and 24 oz; Market Basket Cottage Cheese with Pineapple, 16 oz; Penn Maid Cottage Cheese with Pineapple, 16 oz;

Quantity

391,824 cases (total)

Reason

Product may contain foreign objects (plastic).

Recall initiation date

October 25, 2022

Report date

November 9, 2022

Classification date

Not published in this source record

Termination date

March 1, 2023

Distribution pattern

Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Mexico, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, Texas, Utah, Vermont, Virginia, Washington, Wisconsin, Wyoming

UPC, lot, and code information

Products being recalled have a best by date between Oct 24 2022 through Dec 12 2022

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 91053 with 10 other product entries in Public Health Trace.

Responsible company: HP Hood LLC

Other recalls from HP Hood LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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